ES8603409A1 - Process for making 2-oxindole-1-carboxamides and intermediates therefor. - Google Patents
Process for making 2-oxindole-1-carboxamides and intermediates therefor.Info
- Publication number
- ES8603409A1 ES8603409A1 ES541373A ES541373A ES8603409A1 ES 8603409 A1 ES8603409 A1 ES 8603409A1 ES 541373 A ES541373 A ES 541373A ES 541373 A ES541373 A ES 541373A ES 8603409 A1 ES8603409 A1 ES 8603409A1
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- optionally substituted
- oxindole
- carboxamides
- making
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000543 intermediate Substances 0.000 title abstract 2
- UYINJAQCJCYCGO-UHFFFAOYSA-N 2-oxo-3h-indole-1-carboxamide Chemical class C1=CC=C2N(C(=O)N)C(=O)CC2=C1 UYINJAQCJCYCGO-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- WVKPYYLOFMTDHB-UHFFFAOYSA-N 2-norbornyl radical Chemical group C1CC2[CH]CC1C2 WVKPYYLOFMTDHB-UHFFFAOYSA-N 0.000 abstract 1
- PCKPVGOLPKLUHR-UHFFFAOYSA-N OH-Indolxyl Natural products C1=CC=C2C(O)=CNC2=C1 PCKPVGOLPKLUHR-UHFFFAOYSA-N 0.000 abstract 1
- -1 bicyclo[2.2.1]hept-5-en-2-yl Chemical group 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical compound C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/38—Oxygen atoms in positions 2 and 3, e.g. isatin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Covers oxindole intermediates, and their preparation, of the formula: < CHEM > wherein X and Y are certain stated substituents or may when taken together form certain ring structures, and R is H or -COR<1> where R<1> is alkyl, cycloalkyl, cycloalkenyl, optionally substituted phenyl, optionally substituted phenylalkyl, optionally substituted phenoxyalkyl, (thiophenoxy)alkyl, naphthyl, bicyclo[2.2.1]heptan-2-yl, bicyclo[2.2.1]hept-5-en-2-yl or -(CH2)n-Q-R where n is 0, 1 or 2, Q is a divalent radical which is a specified heterocycle, and R<0> is H or alkyl and also covers the hydrolysis of the compounds (II) to end products of the formula: < CHEM > r
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59066784A | 1984-03-19 | 1984-03-19 | |
| US68488984A | 1984-12-21 | 1984-12-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES541373A0 ES541373A0 (en) | 1985-12-16 |
| ES8603409A1 true ES8603409A1 (en) | 1985-12-16 |
Family
ID=27080914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES541373A Expired ES8603409A1 (en) | 1984-03-19 | 1985-03-18 | Process for making 2-oxindole-1-carboxamides and intermediates therefor. |
Country Status (29)
| Country | Link |
|---|---|
| EP (1) | EP0155828B1 (en) |
| JP (1) | JPH03178963A (en) |
| KR (1) | KR860001874B1 (en) |
| AR (1) | AR247885A1 (en) |
| AU (1) | AU552119B2 (en) |
| BG (1) | BG44203A3 (en) |
| CA (1) | CA1250832A (en) |
| CS (1) | CS250680B2 (en) |
| CY (1) | CY1667A (en) |
| DE (1) | DE3579716D1 (en) |
| DK (2) | DK163662C (en) |
| EG (1) | EG17274A (en) |
| ES (1) | ES8603409A1 (en) |
| FI (1) | FI85265C (en) |
| GR (1) | GR850669B (en) |
| HK (1) | HK75992A (en) |
| HU (1) | HU194825B (en) |
| IE (1) | IE57741B1 (en) |
| IL (1) | IL74630A (en) |
| MA (1) | MA20379A1 (en) |
| NO (1) | NO168639C (en) |
| NZ (1) | NZ211487A (en) |
| OA (1) | OA07967A (en) |
| PH (1) | PH20843A (en) |
| PL (1) | PL145873B1 (en) |
| PT (1) | PT80116B (en) |
| RO (1) | RO90953B (en) |
| YU (1) | YU43869B (en) |
| ZW (1) | ZW4885A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0153818B1 (en) * | 1984-02-07 | 1989-03-15 | Pfizer Inc. | 1,3-disubstituted 2-oxindoles as analgesic and anti-inflammatory agents |
| US4686224A (en) * | 1984-10-31 | 1987-08-11 | Pfizer Inc. | Oxindole antiinflammatory agents |
| DE3621761A1 (en) * | 1986-06-28 | 1988-01-07 | Bayer Ag | INDOLYL PROPIONIC ACIDS |
| RO105052B1 (en) * | 1987-02-02 | 1994-12-01 | Pfizer | Producing process for the crystalline sodium salt, anhydre, of 5-chlorine-3-(2-tenoil)-2-oxindol-1-carboxamide |
| GB8720693D0 (en) * | 1987-09-03 | 1987-10-07 | Glaxo Group Ltd | Chemical compounds |
| US4952703A (en) * | 1989-05-25 | 1990-08-28 | Pfizer Inc. | Intermediates for making 2-oxindole-1-carboxamides |
| HUP9600855A3 (en) * | 1996-04-03 | 1998-04-28 | Egyt Gyogyszervegyeszeti Gyar | Process for producing tenidap |
| JP2004529110A (en) | 2001-03-06 | 2004-09-24 | アストラゼネカ アクチボラグ | Indole derivatives with vascular damage activity |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3767653A (en) * | 1971-06-28 | 1973-10-23 | Squibb & Sons Inc | Thiazines |
-
1985
- 1985-03-15 EP EP85301807A patent/EP0155828B1/en not_active Expired - Lifetime
- 1985-03-15 CA CA000476599A patent/CA1250832A/en not_active Expired
- 1985-03-15 IE IE683/85A patent/IE57741B1/en not_active IP Right Cessation
- 1985-03-15 GR GR85850669A patent/GR850669B/el not_active IP Right Cessation
- 1985-03-15 DE DE8585301807T patent/DE3579716D1/en not_active Expired - Lifetime
- 1985-03-15 PT PT80116A patent/PT80116B/en unknown
- 1985-03-17 EG EG173/85A patent/EG17274A/en active
- 1985-03-18 YU YU428/85A patent/YU43869B/en unknown
- 1985-03-18 HU HU85993A patent/HU194825B/en unknown
- 1985-03-18 PL PL1985252433A patent/PL145873B1/en unknown
- 1985-03-18 NO NO851059A patent/NO168639C/en not_active IP Right Cessation
- 1985-03-18 ZW ZW48/85A patent/ZW4885A1/en unknown
- 1985-03-18 KR KR1019850001747A patent/KR860001874B1/en not_active Expired
- 1985-03-18 NZ NZ211487A patent/NZ211487A/en unknown
- 1985-03-18 AR AR85299771A patent/AR247885A1/en active
- 1985-03-18 FI FI851068A patent/FI85265C/en not_active IP Right Cessation
- 1985-03-18 IL IL74630A patent/IL74630A/en not_active IP Right Cessation
- 1985-03-18 ES ES541373A patent/ES8603409A1/en not_active Expired
- 1985-03-18 MA MA20603A patent/MA20379A1/en unknown
- 1985-03-18 BG BG069279A patent/BG44203A3/en unknown
- 1985-03-18 AU AU40058/85A patent/AU552119B2/en not_active Expired
- 1985-03-18 DK DK121485A patent/DK163662C/en not_active IP Right Cessation
- 1985-03-19 PH PH32005A patent/PH20843A/en unknown
- 1985-03-19 CS CS851921A patent/CS250680B2/en unknown
- 1985-03-19 RO RO118054A patent/RO90953B/en unknown
- 1985-03-19 OA OA58542A patent/OA07967A/en unknown
-
1990
- 1990-11-30 JP JP2336861A patent/JPH03178963A/en active Granted
-
1991
- 1991-04-11 DK DK064591A patent/DK165179C/en not_active IP Right Cessation
-
1992
- 1992-10-01 HK HK759/92A patent/HK75992A/en not_active IP Right Cessation
-
1993
- 1993-05-14 CY CY1667A patent/CY1667A/en unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD1A | Patent lapsed |
Effective date: 20040823 |